mito-mScarlet
(Plasmid
#141153)
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PurposeFluorescent labeling of the mitochondrial matrix in mammalian cells
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 141153 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepAcGFP-N1
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Backbone manufacturerClontech
- Backbone size w/o insert (bp) 4664
- Total vector size (bp) 4730
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Vector typeMammalian Expression
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Selectable markersNeomycin (select with G418)
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameCOX4
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Alt namepre-CoxIV
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SpeciesS. cerevisiae (budding yeast)
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Insert Size (bp)66
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GenBank IDNM_001181052
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Entrez GeneCOX4 (a.k.a. YGL187C)
- Promoter CMV
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Tag
/ Fusion Protein
- mScarlet (C terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NheI (not destroyed)
- 3′ cloning site BamHI (not destroyed)
- 5′ sequencing primer CMV Forward
- 3′ sequencing primer pFastBac Reverse (Common Sequencing Primers)
Resource Information
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Supplemental Documents
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.
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For your Materials & Methods section:
mito-mScarlet was a gift from Gia Voeltz (Addgene plasmid # 141153 ; http://n2t.net/addgene:141153 ; RRID:Addgene_141153) -
For your References section:
Fission and fusion machineries converge at ER contact sites to regulate mitochondrial morphology. Abrisch RG, Gumbin SC, Wisniewski BT, Lackner LL, Voeltz GK. J Cell Biol. 2020 Apr 6;219(4). pii: 133843. doi: 10.1083/jcb.201911122. 10.1083/jcb.201911122 PubMed 32328629